News from CVM
FDA Seeking Public Input on Animal Drug User Fee Act Information Collection
FDA Takes Significant Steps to Address Antimicrobial Resistance
FDA Addresses Continued Shortage of Drug Used to Treat Heartworm Infection in Dogs
CVM Clarifies Use of Melengestrol Acetate in Combination with Monensin and Tylosin, and with Monensin Alone, in Animal Feed
Veterinary Medication Errors webpage available Food Safety Modernization Act and Animal FeedFood Safety Modernization Act and Animal Feed –
FDA is extending the comment period for:
Proposed Rule: Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals
Draft Qualitative Risk Assessment: Risk of Activity/Animal Food Combinations for Activities (Outside the Farm Definition) Conducted in a Facility Co-Located on a Farm
Annual Report to Congress on the Use of Mandatory Recall Authority Available. Have you ever wondered ....
What is the Green Book?
The Generic Animal Drug and Patent Restoration act requires that each sponsor of an approved animal drug must submit to the FDA certain information regarding patents held for the animal drug or its method of use. The Act requires that this information, as well as a list of all animal drug products approved for safety and effectiveness, be made available to the public. This list must be updated monthly under the provisions of the Act. The list, known as the "Green Book," was first published in January 1989. Updates have been added monthly since then. Each January, the list is published in its entirety.
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